Webinar

In this webinar, gain an in-depth understanding of regulatory and clinical development challenges for rare/orphan diseases.

Learn key processes and tools for your team to use to ensure your organization operates at peak performance.

Clinical decision support (CDS) software is a challenging regulatory space. Conquer the confusion with this roundtable discussion.

Clinical trial costs vary from each site, and a prolonged budget negotiation process can affect the startup timeline.

This webinar will cover successful strategies for a proactive approach to FDA inspections before, during, and after.

Understand the unique regulatory, clinical, and manufacturing requirements for cell and gene therapy research.

Learn successful strategies for a stepwise implementation of a clinical QMS, tailored to companies in growth mode.

Explore tools and metrics designed to best measure site performance and engagement on a macro and micro level.

This webinar offers insights to your pressing questions related to single IRBs and explores the key features of federal sIRB mandates.

Join colleagues from NCI-designated cancer centers to discuss the unique ways oncology has pioneered clinical trial advancements.

A practical discussion of budgeting considerations for sIRB review, including strategies for policies around external IRB reliance.

Explore the latest strategies to accelerate your medical device throughout the product development lifecycle.